Role OverviewWe are looking for an experienced Commissioning, Qualification & Validation (CQV) Engineer to support validation activities within a highly regulated pharmaceutical manufacturing environment.In this role, you will contribute to the commissioning, qualification, and validation of equipment, systems, and facilities, ensuring compliance with cGMP requirements and industry regulations.You will collaborate closely with engineering, quality, and ope
Role OverviewWe are looking for an experienced Commissioning, Qualification & Validation (CQV) Engineer to support validation activities within a highly regulated pharmaceutical manufacturing environment.In this role, you will contribute to the commissioning, qualification, and validation of equipment, systems, and facilities, ensuring compliance with cGMP requirements and industry regulations.You will collaborate closely with engineering, quality, and ope
Title: Quality SpecialistLocation: Visp, Valais, Switzerland (On-site)We are looking for a Quality Specialist with experience in deviation investigations and CAPA management within a GMP-regulated environment – ideally with strong knowledge of processes related to monoclonal antibodies.This role is critical to ensuring regulatory compliance, preventing recurring issues, and strengthening the quality system through effective corrective and preventive action
Title: Quality SpecialistLocation: Visp, Valais, Switzerland (On-site)We are looking for a Quality Specialist with experience in deviation investigations and CAPA management within a GMP-regulated environment – ideally with strong knowledge of processes related to monoclonal antibodies.This role is critical to ensuring regulatory compliance, preventing recurring issues, and strengthening the quality system through effective corrective and preventive action
Are you the person who actually enjoys the adrenaline of a surprise inspection? Do you find the "missing link" in a paper trail before anyone else even realizes it’s gone?Our client, a Randstad client, is looking for a Senior QMS & Compliance Expert to join their team in Visp. We need someone who treats Auditing as an art form, Compliance as a religion, and the Quality Management System (QMS) as their personal masterpiece.If you can stare down a regulatory
Are you the person who actually enjoys the adrenaline of a surprise inspection? Do you find the "missing link" in a paper trail before anyone else even realizes it’s gone?Our client, a Randstad client, is looking for a Senior QMS & Compliance Expert to join their team in Visp. We need someone who treats Auditing as an art form, Compliance as a religion, and the Quality Management System (QMS) as their personal masterpiece.If you can stare down a regulatory
Anstellungsart: Festanstellung bei einem Kunden von RandstadArbeitsort: Visp (100% vor Ort)Arbeitszeit: Wöchentlich wechselndes 3-Schicht-Modell (Montag – Freitag, keine Wochenendarbeit)Ihre Aufgaben:Anlagenbedienung: Überwachung und Bedienung der Abfüllanlage für flüssige pharmazeutische Produkte unter Einhaltung höchster Qualitätsstandards.Isolator-Tätigkeiten: Durchführung spezialisierter Aufgaben am Isolator im Rahmen der sterilen Abfüllung.Logistik &
Anstellungsart: Festanstellung bei einem Kunden von RandstadArbeitsort: Visp (100% vor Ort)Arbeitszeit: Wöchentlich wechselndes 3-Schicht-Modell (Montag – Freitag, keine Wochenendarbeit)Ihre Aufgaben:Anlagenbedienung: Überwachung und Bedienung der Abfüllanlage für flüssige pharmazeutische Produkte unter Einhaltung höchster Qualitätsstandards.Isolator-Tätigkeiten: Durchführung spezialisierter Aufgaben am Isolator im Rahmen der sterilen Abfüllung.Logistik &
Location: Switzerland (100% on-site)Contract type: Full-timeLanguage: German (mandatory); English a strong plusThe roleJoin a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ protocols, and deliver audit-ready documentation in line with cGMP/GxP and internal procedures.What you’ll doPlan and coordinate CQV for facilities & utilities
Location: Switzerland (100% on-site)Contract type: Full-timeLanguage: German (mandatory); English a strong plusThe roleJoin a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ protocols, and deliver audit-ready documentation in line with cGMP/GxP and internal procedures.What you’ll doPlan and coordinate CQV for facilities & utilities
Senior Bioprocess Engineer (Biologics)Location: Visp, Switzerland — 100% on-siteFunction: Operations / Manufacturing Science & Technology (MSAT)Type: Full-time, permanent (immediate start possible)The opportunityA fast-growing biologics site is expanding its Microbial / Mammalian / BioConjugates operations. We’re looking for an experienced Senior Bioprocess Engineer who can lead change on the shopfloor—owning operational readiness, documentation updates, a
Senior Bioprocess Engineer (Biologics)Location: Visp, Switzerland — 100% on-siteFunction: Operations / Manufacturing Science & Technology (MSAT)Type: Full-time, permanent (immediate start possible)The opportunityA fast-growing biologics site is expanding its Microbial / Mammalian / BioConjugates operations. We’re looking for an experienced Senior Bioprocess Engineer who can lead change on the shopfloor—owning operational readiness, documentation updates, a
About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,
About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,